290 research outputs found

    Les besoins et les enjeux en matiĂšre d’analyse criminelle stratĂ©gique et opĂ©rationnelle

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    Cette table ronde fait suite Ă  la Recommandation n° 24 du Vademecum : promouvoir des travaux de recherche acadĂ©mique in loco au sein de services de police/gendarmerie (soit en tant qu’officier de police/chercheur, soit en tant que chercheur rĂ©sident) pour accĂ©der plus facilement aux donnĂ©es dans un environnement sĂ©curisĂ© et diffuser de nouvelles mĂ©thodes, de nouvelles approches etc. entre pairs. Ces initiatives seraient particuliĂšreÂŹment importantes pour faciliter les recherches acadĂ©miques pour, avec et par des praticiens, qui permettent d’injecter l’expĂ©rience dans un processus intellectuel

    Une offre de services adaptée aux chercheurs

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    Ayant l'un des groupes de lecteurs les plus exigeants dans le monde scientifique et des ressources comparables Ă  celles d'une collection de moyenne bibliothĂšque universitaire, le Service de l'Information Scientifique du CERN utilise toute sa crĂ©ativitĂ© pour ne pas disparaĂźtre entre l'offre et la demande. Le CERN a pour but d'ĂȘtre un centre d'excellence dans le domaine de la physique des hautes energies et des technologies connexes. Le Service d'Information Scientifique rĂ©alise cet objectif en prĂ©servant la mĂ©moire des dĂ©veloppements de la physique et en appliquant les technologies avancĂ©es des sciences de l'information et du commerce Ă©lectronique

    Entérite hémorragique du Porc

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    Servettaz Jean. Entérite hémorragique du Porc. In: Bulletin de l'Académie Vétérinaire de France tome 104 n°1, 1951. pp. 66-69

    Rouget du Porc. Actions thérapeutiques du sérum et de la pénicilline

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    Chez le Porc, dans le traitement du rouget, le sĂ©rum spĂ©cifique employĂ© judicieusement, injectĂ© d’emblĂ©e Ă  forte dose, se suffit toujours Ă  lui-mĂȘme. Il est tout Ă  fait inutile de lui adjoindre un sulfamidĂ© ou un antibiotique, et la pĂ©nicilline ne paraĂźt avoir aucun degrĂ© d’efficacitĂ©. Le rouget n’est pas contagieux ; il apparaĂźt sous l’influence de causes favo risantes qui nous Ă©chappent le plus souvent, mais qui parfois se laissent discerner, exemples : la vaccination anti-aphteuse (Servettaz) , la vacci nation contre la peste par le vaccin au cristal violet

    Effect of oxidative stress on protein tyrosine phosphatase 1B in scleroderma dermal fibroblasts

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    Objective Platelet‐derived growth factor (PDGF) and its receptor, PDGFR, promote fibrosis in systemic sclerosis (SSc; scleroderma) dermal fibroblasts, and such cells in scleroderma skin lesions produce excessive reactive oxygen species (ROS). PDGFR is phosphorylated upon PDGF stimulation, and is dephosphorylated by protein tyrosine phosphatases (PTPs), including PTP1B. This study was undertaken to determine whether the thiol‐sensitive PTP1B is affected by ROS in SSc dermal fibroblasts, thereby enhancing the phosphorylation of PDGFR and synthesis of type I collagen. This study also sought to investigate the effect of a thiol antioxidant, N ‐acetylcysteine (NAC), in SSc. Methods Fibroblasts were isolated from the skin of patients with diffuse SSc and normal healthy donors for cell culture experiments and immunofluorescence analyses. A phosphate release assay was used to determine the activity of PTP1B. Results Levels of ROS and type I collagen were significantly higher and amounts of free thiol were significantly lower in SSc fibroblasts compared to normal fibroblasts. After stimulation with PDGF, not only were PDGFR and ERK‐1/2 phosphorylated to a greater extent, but also the ability to produce PTP1B was hampered in SSc fibroblasts. The activity of PTP1B was significantly inactivated in SSc fibroblasts as a result of cysteine oxidation by the raised levels of ROS, which was confirmed by the oxidation of multiple PTPs, including PTP1B, in SSc fibroblasts. Decreased expression of PTP1B in normal fibroblasts led to increased expression of type I collagen. Treatment of the cells with NAC restored the activity of PTP1B, improved the profile of PDGFR phosphorylation, decreased the numbers of tyrosine‐phosphorylated proteins and levels of type I collagen, and scavenged ROS in SSc fibroblasts. Conclusion This study describes a new mechanism by which ROS may promote a profibrotic phenotype in SSc fibroblasts through the oxidative inactivation of PTP1B, leading to pronounced activation of PDGFR. The study also presents a novel molecular mechanism by which NAC may act on ROS and PTP1B to provide therapeutic benefit in SSc.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/91336/1/34336_ftp.pd

    Diagnostic Utility of Separate Anti-Ro60 and Anti-Ro52/TRIM21 Antibody Detection in Autoimmune Diseases

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    Anti-SS-A antibodies are often sought for in autoimmune diseases diagnosis. Two different target proteins have actually been identified: Ro52 and Ro60. Clinical and immunological associations seem different depending on anti-Ro52 or anti-Ro60 antibodies presence. However, due to a heterogeneous presentation in the literature, some immunology laboratories in France have stopped providing anti-Ro52 antibody findings. We report here a new hospital study designed to determine the diagnostic utility of the separate detection of anti-Ro52 and anti-Ro60 antibodies. We conducted a retrospective, observational study, including every adult patient with positive antinuclear antibodies (ANA) tested in our immunology laboratory, and associated with anti-Ro52 and/or anti-Ro60 antibodies, between 2011 and 2014. Out of 13032 sera tested for ANA, 399 adults had antibodies to Ro52 and/or Ro60; 81.7% were female, with a mean age of 54.5 ± 17.0 years. Anti-Ro52 antibodies were found in 75.7% of the patients and anti-Ro60 antibodies in 56.9%. Among them, 43.1% were classified in the Ro52 + Ro60- group, 32.6% in the Ro52 + Ro60 + group and 24.3% in the Ro52-Ro60+ group. In the Ro52-Ro60+ group, systemic lupus was the most frequent diagnosis (48.5%), with a possible association with antiphospholipid antibodies (anti-cardiolipin antibodies: OR 2.5 (CI95 [1.0–5.0], p = 0.05) and lupus anticoagulant {OR 3.6 (CI95 [1.10–10.0] p = 0.02)}. In the Ro52+Ro60+, primary Sjögren Syndrome was the most likely (OR 4.2 95% CI [2.1–8.3] p < 10−4), especially in patients Ro52+Ro60+La+. Patients with isolated anti-Ro52 had a wider variety of diseases associated, but among auto-immune diseases they were more prone to inflammatory myositis (OR 10.5 [1.4–81.7], p = 0.02) and inflammatory rheumatism (OR 4.6 [1.6–13.8], p = 0.006) in contrast to systemic lupus (OR 0.2 [0.1–0.3], p < 10−4) or primary Sjögren's syndrome (OR 0.1 [0.06–0.2], p < 10−4). We therefore suggest that, when anti-ENA antibodies are prescribed, it should include separate anti-Ro52 and anti-Ro60 antibodies determination. To go even further, we would like to suggest a change in ENA nomenclature to avoid confusion, abandoning the anti-SS-A label in favor of the anti-Ro52/TRIM21 or anti-Ro60 antibody for a clearer designation

    The natural organosulfur compound dipropyltetrasulfide prevents HOCL-induced systemic sclerosis in the mouse

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    PublishedArticleIntroduction: The aim of this study was to test the naturally occurring organosulfur compound dipropyltetrasulfide (DPTTS) found in plants, which has antibiotic and anti-cancer properties, as a treatment of HOCl-induced systemic sclerosis in the mouse. Methods: The pro-oxidative, anti-proliferative and cytotoxic effects of DPTTS were evaluated ex vivo on fibroblasts from normal and HOCl-mice. In vivo, the anti-fibrotic and immunomodulating properties of DPTTS were evaluated in the skin and lungs of HOCl-mice. Results: H2O2 production was higher in fibroblasts derived from HOCl-mice than in normal fibroblasts (P<0.05). DPTTS did not increase H2O2 production in normal fibroblasts, but DPTTS dose-dependently increased H2O2 production in HOCl-fibroblasts (P<0.001 with 40ÎŒM DPTTS). Because H2O2 reached a lethal threshold in cells from HOCl-mice, the anti-proliferative, cytotoxic and pro-apoptotic effects of DPTTS were significantly higher in HOCl-fibroblasts than for normal fibroblasts. In vivo, DPTTS decreased dermal thickness (P<0.001), collagen content in skin (P<0.01) and lungs (P<0.05), SMA (P<0.01) and pSMAD2/3 (P<0.01) expression in skin, formation of advanced oxidation protein products and anti-DNA topoisomerase-1 antibodies in serum (P<0.05) versus untreated HOCl- mice. Moreover, in HOCl-mice, DPTTS reduced splenic B cell counts (P<0.01), the proliferative rates of B-splenocytes stimulated by lipopolysaccharide (P<0.05) and T-splenocytes stimulated by anti-CD3/CD28 mAb (P<0.001). Ex vivo, it also reduced the production of IL-4 and IL-13 by activated T cells (P<0.05 in both cases). Conclusions: The natural organosulfur compound DPTTS prevents skin and lung fibrosis in the mouse through the selective killing of diseased fibroblasts and its immunomodulating properties. DPTTS may be a potential treatment of Systemic sclerosis.This work was supported by European Community’s Seventh Framework Programme (FP7/2007-2013) under grant agreement 215009 RedCat for financial support. The authors are grateful to Ms Agnes for her excellent typing of the manuscript

    Is Aphtous Oral Ulceration Biopsy always Useless?

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    Objective: To report a case of Behçet’s disease whose diagnosis was only confirmed thanks to an oral aphthous lesion biopsy. Materials and methods: Conventional histopathological analysis of a biopsy of an aphthous oral lesion that had appeared two days previously. Results: A small vein vasculitis with eosinophil and neutrophil granulocytes was evidenced. Conclusion: The presence of a small vein vasculitis was here strongly in favour of Behçet's disease, whereas such a diagnosis was not confirmed according to the International Study Group’s criteria
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